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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myxofibrosarcoma
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit

CREB3L1 WWOX
CREB3L2
FUS


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FUS
(0.63)
WWOX



Citations in the biomedical literature:


Myxofibrosarcoma
CREB3L1 CREB3L2 FUS
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
WWOX



Myxofibrosarcoma
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit

Synonym(s):
- Fibromyxosarcoma
- Myxoid malignant fibrous histiocytoma

Synonym(s):
- Autosomal recessive spinocerebellar ataxia-12
- SCAR12

Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.